Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Karolina Tiara"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 634-641 (2018)
An efficient methodology for the selective substitution of both terminal positions (C6 and C6’) in 1’,2,3,3’,4,4’-hexa-O-benzylsucrose with different unsaturated monosaccharide units is presented. Such a highly functionalized intermediate was
Externí odkaz:
https://doaj.org/article/32d859074114487e9993b60c427db93f
Autor:
Grzegorz Witkowski, Mykhaylo A. Potopnyk, Karolina Tiara, Anna Osuch-Kwiatkowska, Sławomir Jarosz
Publikováno v:
Molecules, Vol 25, Iss 15, p 3357 (2020)
2,3,4-Tri-O-benzyl-D-xylopyranose was used as a starting material in the preparation of the corresponding triene, which underwent smooth cyclization to a polyhydroxylated hydrindane, as a single diastereoisomer. The analogous triene prepared from D-g
Externí odkaz:
https://doaj.org/article/736f8d85d6bb48d29402ae4b0cbe8d72
Publikováno v:
Arkivoc. 2021:105-112
Publikováno v:
Pure and Applied Chemistry. 91:1137-1148
A number of bicyclic imino- and carba-sugars (examples are presented in the Scheme) can be obtained from simple monosaccharides (hexoses or pentoses) by various methods.
Autor:
Karolina Tiara, Mykhaylo A. Potopnyk, Sławomir Jarosz, Anna Osuch-Kwiatkowska, Grzegorz Witkowski
Publikováno v:
Molecules
Volume 25
Issue 15
Molecules, Vol 25, Iss 3357, p 3357 (2020)
Volume 25
Issue 15
Molecules, Vol 25, Iss 3357, p 3357 (2020)
2,3,4-Tri-O-benzyl-D-xylopyranose was used as a starting material in the preparation of the corresponding triene, which underwent smooth cyclization to a polyhydroxylated hydrindane, as a single diastereoisomer. The analogous triene prepared from D-g
Publikováno v:
The Journal of Organic Chemistry
A highly efficient methodology of the preparation of synthetically important tetrahydrofuran derivatives with an amino substituent in the side chain is reported. This process is based on the stereocontrolled debenzylative cycloetherification (DBCE) r
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 634-641 (2018)
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 634-641 (2018)
An efficient methodology for the selective substitution of both terminal positions (C6 and C6’) in 1’,2,3,3’,4,4’-hexa-O-benzylsucrose with different unsaturated monosaccharide units is presented. Such a highly functionalized intermediate was